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一例罕见的原发性腹膜后黏液性囊腺癌伴复发性感染性腰大肌脓肿。

A rare case of primary retroperitoneal mucinous cystadenocarcinoma presenting with recurrent infected psoas abscess.

作者信息

Hamza Hafiz Muhammad, Khan Naveed Ullah, Tariq Muhammad Daoud, Malik Muhammad Muiz, Awan Ayaz Ahmed, Sharma Umang

机构信息

Department of Surgery, Foundation University School of Health Sciences, Islamabad, Pakistan.

HOD Surgical Unit, Federal Government Polyclinic Hospital Islamabad, Islamabad, Pakistan.

出版信息

Ann Med Surg (Lond). 2025 Jun 24;87(9):6052-6056. doi: 10.1097/MS9.0000000000003494. eCollection 2025 Sep.

Abstract

INTRODUCTION AND SIGNIFICANCE

Retroperitoneal mucinous adenocarcinoma is a rare malignancy, typically presenting with nonspecific symptoms leading to delay in diagnosis and treatment.

CASE PRESENTATION

A 53-year-old man patient was seen with debilitating pain in the right thigh and reduced mobility, following 1 year of recurrent psoas abscesses. The physical exam revealed a mass in the right flank and a positive psoas sign. The laboratory work revealed elevated alkaline phosphatase and carcinoembryonic antigen (CEA), with decreased hemoglobin and creatine phosphokinase. Imaging revealed a large heterogeneous retroperitoneal mass (25.88 × 17.44 × 17.26 cm) compressing adjacent structures. Drainage was mucinous in nature; histopathology revealed well-differentiated mucinous adenocarcinoma with cytokeratin positivity. infection proved secondary contamination from gastrointestinal sources. Antibiotics, analgesics, and interval drainage were administered to the patient. Chemotherapy was considered but later contraindicated with the onset of renal failure. The patient was placed on palliative care with symptomatic improvement.

CLINICAL DISCUSSION

This case highlights the diagnostic difficulty of retroperitoneal mucinous adenocarcinoma, especially when occulted by infection and nonspecific presentation. The secondary infection and massive size of the tumor contribute to the difficulty in diagnosis and treatment.

CONCLUSION

Early detection through thorough assessment is paramount. Multidisciplinary management is indicated, although such complications as renal failure may interfere with treatment and decrease prognosis.

摘要

引言与意义

腹膜后黏液腺癌是一种罕见的恶性肿瘤,通常表现为非特异性症状,导致诊断和治疗延迟。

病例介绍

一名53岁男性患者,在反复出现腰大肌脓肿1年后,出现右大腿剧痛且活动能力下降。体格检查发现右腹侧有肿块,腰大肌征阳性。实验室检查显示碱性磷酸酶和癌胚抗原(CEA)升高,血红蛋白和肌酸磷酸激酶降低。影像学检查显示一个巨大的异质性腹膜后肿块(25.88×17.44×17.26 cm)压迫相邻结构。引流液呈黏液性;组织病理学显示为高分化黏液腺癌,细胞角蛋白呈阳性。感染被证明是胃肠道来源的继发性污染。给予患者抗生素、镇痛药和间歇性引流。考虑过化疗,但后来因肾衰竭的发生而禁忌。患者接受姑息治疗,症状有所改善。

临床讨论

该病例突出了腹膜后黏液腺癌的诊断困难,尤其是当被感染和非特异性表现掩盖时。肿瘤的继发性感染和巨大体积导致诊断和治疗困难。

结论

通过全面评估进行早期检测至关重要。尽管肾衰竭等并发症可能干扰治疗并降低预后,但仍需多学科管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09c6/12401258/ec319441d1ea/ms9-87-6052-g001.jpg

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